Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 4:155510693 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM921008

Most severe consequence
Clinical significance

Synonyms

LSDB 1923

This variation has 5 HGVS names - click the plus to show

4:g.155510693C>T
ENST00000302053.3:c.76G>A
ENSP00000306361.3:p.Asp26Asn
ENST00000403106.3:c.76G>A
ENSP00000385981.3:p.Asp26Asn

Variation displays